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Cell-type-specific splicing of transcription regulators and Ptbp1 by Rbfox1/2/3 in the developing neocortex.
Ruan, Xiangbin; Hu, Kaining; Yang, Yalan; Yang, Runwei; Tseng, Elizabeth; Kang, Bowei; Kauffman, Aileen; Zhong, Rong; Zhang, Xiaochang.
Afiliación
  • Ruan X; Department of Human Genetics, The University of Chicago, Chicago, IL 60637, USA.
  • Hu K; Equal contributions.
  • Yang Y; Department of Human Genetics, The University of Chicago, Chicago, IL 60637, USA.
  • Yang R; Equal contributions.
  • Tseng E; Department of Human Genetics, The University of Chicago, Chicago, IL 60637, USA.
  • Kang B; Equal contributions.
  • Kauffman A; Department of Human Genetics, The University of Chicago, Chicago, IL 60637, USA.
  • Zhong R; Pacific Biosciences, Menlo Park, CA 94025, USA.
  • Zhang X; Department of Human Genetics, The University of Chicago, Chicago, IL 60637, USA.
bioRxiv ; 2024 Sep 10.
Article en En | MEDLINE | ID: mdl-39314274
ABSTRACT
How master splicing regulators crosstalk with each other and to what extent transcription regulators are differentially spliced remain unclear in the developing brain. Here, cell-type-specific RNA-Seq of the developing neocortex uncover that transcription regulators are enriched for differential splicing, altering protein isoforms or inducing nonsense-mediated mRNA decay. Transient expression of Rbfox proteins in radial glia progenitors induces neuronal splicing events preferentially in transcription regulators such as Meis2 and Tead1. Surprisingly, Rbfox proteins promote the inclusion of a mammal-specific alternative exon and a previously undescribed poison exon in Ptbp1. Simultaneous ablation of Rbfox1/2/3 in the neocortex downregulates neuronal isoforms and disrupts radial neuronal migration. Furthermore, the progenitor isoform of Meis2 promotes Tgfb3 transcription, while the Meis2 neuron isoform promotes neuronal differentiation. These observations indicate that transcription regulators are differentially spliced between cell types in the developing neocortex.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos